US EPA

7479483 

Journal Article 

Oxime carbamates as potential insecticidal agents: Design, synthesis and biological evaluation 

Ke, S; Yang, Z; Shi, L; Liu, M; Liang, Y; Wang, K; Long, T; Jiang, A; Zhang, Z 

2015 

1 

Letters in Drug Design & Discovery
ISSN: 1570-1808 

Bentham Science Publishers B.V. 

12 

9 

771-777 

English 

10.2174/1570180812666150429234510 

A series of oxime carbamates derivatives were designed and synthesized as a part of our ongoing search for novel high potential agrochemicals. Their structures were confirmed by 1H NMR, 13C NMR and elemental analysis. The bioassays results indicated that some of the obtained compounds exhibited good insecticidal activity against Heliothis armigera and Plutella xylostella. © 2015 Bentham Science Publishers. 

Insecticidal activity; Oxime carbamates; Synthesis; 1 p tolylethanone o 4 chlorophenylcarbamoyl oxime; 2 chlorobenzaldehyde o 4 chlorophenylcarbamoyl oxime; 2 fluorobenzaldehyde o 4 chlorophenylcarbamoyl oxime; 3,4,5 trimethoxybenzaldehyde o 4 chlorophenylcarbamoyl oxime; 4 (trifluoromethyl)benzaldehyde o 4 (trifluoromethyl)phenylcarbamoyl oxime; 4 (trifluoromethyl)benzaldehyde o 4 chlorophenylcarbamoyl oxime; 4 (trifluoromethyl)benzaldehyde o phenylcarbamothioyl oxime; 4 (trifluoromethyl)benzaldehyde o phenylcarbamoyl oxime; 4 chlorobenzaldehyde o 4 chlorophenylcarbamoyl oxime; 4 chlorobenzaldehyde o phenylcarbamothioyl oxime; 4 fluorobenzaldehyde o 4 (trifluoromethyl)phenylcarbamoyl oxime; 4 fluorobenzaldehyde o 4 chlorophenylcarbamoyl oxime; 4 fluorobenzaldehyde o phenylcarbamothioyl oxime; benzophenone o 4 chlorophenylcarbamoyl oxime; carbamic acid derivative; insecticide; oxime carbamate derivative; oxime derivative; unclassified drug; Article; bioassay; biological activity; carbon nuclear magnetic resonance; clinical evaluation; drug design; drug structure; drug synthesis; Helicoverpa armigera; insecticidal activity; nonhuman; Plutella xylostella; polymerization; priority journal; proton nuclear magnetic resonance; structure analysis